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发表于 2014-2-18 10:07:41
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本帖最后由 xuefeixyg 于 2014-2-18 10:10 编辑
目录
1 Analytical Validation within the Pharmaceutical Environment
2 Performance Parameters, Calculations and Tests
3 Case Study: Validation of an HPLC-Method for Identity, Assay, and Related Impurities
4 Qualification of Analytical Equipment
5 Validation During Drug Product Development – Considerations as a Function of the Stage of Drug Development
6 Acceptance Criteria and Analytical Variability
7 Transfer of Analytical Procedures
8 Validation of Pharmacopoeial Methods
9 Analytical Procedures in a Quality Control Environment
10 Aberrant or Atypical Results
11 Future Trends in Analytical Method Validation
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